NZ201919A

NZ201919A - 2-amino-1,2,3,4-tetrahydronaphthalene derivatives

Info

Publication number: NZ201919A
Application number: NZ201919A
Authority: NZ
Inventors: N Beeley; M Dimsdale; G Cremer; P Manoury
Original assignee: Synthelabo
Priority date: 1981-09-16
Filing date: 1982-09-15
Publication date: 1985-10-11
Also published as: DK412082A; ZA826770B; IE822249L; IL66804A0; DK163055B; DK163055C; MX158073A; JPS61165324A; EP0074903A2; JPS6121621B2; JPS61165323A; NO154391C; EP0074903B1; ES8403857A1; IL66804A; CA1224491A; NO823125L; EP0074903A3; AU551898B2; ES515744A0

Abstract

New compounds of the formula: <IMAGE> wherein R1 represents a hydrogen atom or an alkanoyl group containing from 1 to 4 carbon atoms, R2 and R3 each represent a hydrogen atom or a C1-C4 alkyl group, and R4 represents a hydroxy or methoxy group in the 6-position or 7-position, have been found to be useful in therapy, and more particularly in the treatment of cardiovascular diseases and Parkinson's disease.

Description

<div class="application article clearfix" id="description"> New Zealand Paient Spedficaiion for Paient Number £01 919 201919 aa nmbms I L>3ieis;: .. j 1 I Complete Specification Filed: J Class: . £.<?. y.^r?!{. i .££.7 C Publication Date: ... It A ,9P^[ .1^)^ P.O. Journal. No: .. !X7(> NEW ZEALAND N,£ 5 6-g^ THE PATENTS ACT 1953 PATENTS FORM NO. 5 COMPLETE SPECIFICATION "2-AMINO-l,2,3,4-TETRAHYDRONAPHTHALENE DERIVATIVES" WE, SYNTHELABO, a French Body Corporate of 7i'^l CeJex 11, 58, rue de la Glaciere, 9-5013 Paris^ France, hereby declare the invention for which we pray that a patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement: 6fol towed by p3G2. \cx) 20/> 1 U Ico- DESCRIPTION "2 AMINO 1,2,3,4 TETRAiriPRONAPIITIIAIjENE DERIVATIVES" The present invention relates to new therapeutically useful 2-amino-l,2,3,4-tetrahydro-naphthalene derivatives, to processes for their preparation and pharmaceutical compositions containing derivatives of the present invention are those compounds of the general formula: 10 wherein R^ represents a hydrogen atom or an alkanoyl group containing from 1 to 4 carbon atoms, R2 and R^ each represent, independently of one another, a hydrogen atom or an alkyl group containing from 1 to 4 carbon atoms, and R^ represents a hydroxy or methoxy group 15 located in the 6-position or 7-position, and their 5 them. The 2-amino-l,2,3,4-tetrahydronaphthalene Rj^-NH (I) 2 DI 2 pharmacologically-acceptable acid addition salts. As the compounds of the invention of general formula (I) contain an asymmetric carbon atom in their molecule (2-position), they can be in the form of 5 racemates or enantiomers. The preferred compounds of the invention are those of general formula (I) wherein represents the formyl (i.e. -CHO) or acetyl (i.e. -COCH^) group, and R.2 and each represent a propyl group, and more especially 10 those compounds in which the group R^ is in the 6-position and the group -NHR^ is in the 5-position. Preferably is the hydroxy group. An outstanding compound of the invention is 2-dipropylamino-5-formylamino-6-hydroxy-1,2,3,4-tetrahydronaphthalene. 15 Those compounds of general formula (I) wherein R-, and R^ iioth represent hydrogen atoms or alkyl groups (viz. the grouping -NR2R2 represents a primary amino or dialkylamino group) can be prepared by reacting 6-methoxy- or 7-methoxy-l,2,3,4-tetrahydro-20 naphthalen-2-one, which are commercially available products, corresponding to the formula: (II) 201919 - 3 - (wherein the rnethoxy group is located in the 6- or 7-position) with benzylamine or a dialkylamine of the general formula: R'2-NH-R*3 (III) 5 (wherein R'2 and R'^ each represent an alkyl group containing from 1 to 4 carbon atoms) to give a 2-amino- 6 (or 7) -me thoxy-3,4-dihydronaphthalene of the general formula: R" (IV) 10 (wherein R"^ represents hydrogen and R"^ represents a benzyl group, or both represent alkyl groups containing from 1 to 4 carbon atc-ns) and hydrogenating such a compound under pressure to give a 2-amino-tetrahydronaphthalene of the general formula: (V) wherein R"2 and R" ^ both represent hydrogen atoms or both represent alkyl groups containing from 1 to 4 carbon atoms, and the methoxy group is located in the 6- or 7-position. 201919 - 4 - The compounds of general formula (V) wherein R"2 and R"^ represent identical alkyl groups can also be obtained by alkylation of a corresponding 2-amino compound of general formula (V) wherein R"^ and R"^ 5 both represent hydrogen atoms. The alkylation can be carried out in a manner known per se, for example by reacting a suspension of an acid addition salt of the primary amine (V) with an appropriate alkyl halide containing 1 to 4 carbon atoms* preferably the iodide, in 10 the presence of a base such as potassium carbonate. This method of preparation is to be preferred when it is desired to prepare a single enantiomer of a compound of general formula (I) wherein R2 and R^ both represent the same alkyl group. In fact, it is easier to separate 15 the enantiomers of the primary amine of general formula (V) (i.e. the grouping -NR^R''^ is -NI^) than the enantiomers of the final compound. The amino compound of general formula (V) is then subjected to nitration. This produces a mixture of 20 two isomers nitrated respectively in the 5-position and 7-position if the methoxy group is in the 6-position, or in the 6-position and 8-position if the methoxy group is in the 7-position, according to the general formula: 2 o i 9 1 9 - 5 - (VI) N02 wherein R'^ and R"^ are as hereinbefore defined# and the methoxy group is located in the 6- or 7-position. The nitro derivatives of the general formula (VI) 5 are new compounds and also form part of the present invention. If desired# one of the nitro derivatives is then demethylated after it has been separated from its isomer# and this gives an acid addition salt of the 10 6(or 7)-hydroxy-2-aminotetrahydronaphthalene of the general formula: (VII) wherein R'^ and R"^ are as hereinbefore defined. Catalytic reduction (Pd# Raney Ni) of the nitro 15 group of the compound of general formula (VI) or (VII) results in the diamine of the general formula: - 6 - 0 u 0>l ?19 (VIII) (wherein R"2* R,,3 an<3 are as hereinbefore defined) which is finally subjected, if desired, to N-acylation by means of an acid of the general formula R'^-OH 5 (wherein R'^ represents an alkanoyl group containing from 1 to 4 carbon atoms), or an acylating derivative thereof, to give a compound of general formula (I). The methods used in the production of the compounds of the invention may be any of those known in the art. The particular methods set out below are by way of example only. The condensation of benzylamine or the dialkylamine of general formula (III) with the tetrahydronaphthalenone of formula (II) can be carried out under the action of heat in a non-polar solvent, such as benzene, in the presence of an acid such as para-toluenesulphonic acid. Hydrogenation of the resulting compound is then carried out in the same reaction vessel in the presence of a hydrogenation catalyst and under pressure. The nitration of the 2-aminotetrahydro-naphthalene of general formula (V) can be carried out in a manner known per se. If the amino group is not alkylated (R"2 and R"3 = H), the amino group should be protected beforehand by acylating it, for example by ' , m ^1,84 Cm sd\ '\Ss « 201^19 - 7 - means of acetic anhydride, and then by removing the acetyl group at the end of the nitration. The two nitro isomers of general formula (VI) are then separated in a known manner, for example by column 5 chromatography. Demethylation of a nitro compound of formula (VI), separated from its isomer, can be carried out, for example, by reaction with hydrobromic acid or by reaction with boron tribromide, followed by salification. 10 The nitro group of the compound of general formula (VII) is then reduced with hydrogen in the presence of a catalyst such as palladium on a carbon support, and also under pressure. Finally, acylation of a compound of general 15 formula (VIII) producing a final compound of general formula (I) wherein R-^ represents an alkanoyl group can be carried out in a known manner, in the cold ice bath, with formic or acetic acid, in the presence of acetic anhydride, or with the anhydride of a higher acid. 20 The compounds of the invention of general formula (I) wherein -NR2R3 denotes a monoalkylamino group can be prepared from a primary amine of general formula (V) (-NR"2R"3 = NH2), in the form of a racemate or an enantiomer. 25 Before carrying out the nitration of the nzene ring, the -NH7 group of the compound of general or ^-1984 019 19 - 8 - formula (V) is acylated, not with any acid as in the case where the final compound of general formula (I) is to have a primary amino group in the 2-position, but by choosing the aliphatic acid* or one of its 5 acylating derivatives, in which the number of carbon atoms corresponds to the length only of the alkyl group 1*2 (or ) of the compound of general formula (I) to be prepared. After the nitration, the separation of the nitro isomers and the reduction of one of them to the 10 primary amine by catalytic hydrogenation, the alkanoyl-amino group in the 2-position is reduced to the monoalkylamino group -NR2R3 (wherein one of the symbols R2 and R^ represents hydrogen and the other represents an alkyl group containing from 1 to 4 carbon atoms), for 15 example with lithium aluminium hydride. Finally, before carrying out the final acylation of the -NH2 group on the benzene ring with an acid R'^-OH (wherein R'^ is as hereinbefore defined) or an acylating derivative thereof, it is possible, if 20 desired, to demethylate the metboxy group in order to obtain a compound of general formula (I) wherein R^ represents the hydroxy group. If it is desired to prepare a compound of general formula (I) in the form of a single enantiomer, 25 irrespective of the group -NR2R3# a step for the .201919 - 9 - separation of the enantiomers of the primary amine of general formula (V) is introduced into the process [in this case, the final compounds of general formula (I) wherein -NI^R^ is a dialkylamino group will be 5 prepared not by reaction of a dialkylamine of general formula (III) with the ketone of formula (II), but by direct alkylation of the separated enantiomer of the primary amine of formula (V)j. The resolution can be carried out by means 10 of the formation of diastereoisomeric salts from chiral acids such as tartaric acid, mandelic acid, camphosulphonic acid and, preferably, dibenzoyltartaric acid. The salification is carried out starting from a 15 mixture of enantiomers of the primary amine of general formula (V), for example starting from the racemate obtained from the ketone of formula (II), in the form of the base, dissolved in a suitable solvent such as an alcohol, preferably ethanol. The two 20 diastereoisomeric salts thus obtained are then separated by fractional crystallisation. After the separation, they can be separated from the chiral acidi that is to say reconverted to the base, and then converted to an addition salt with 25 another acid. n - 10 - An enantiomer of general formula (V) can also be obtained from a base partially enriched in this enantiomeri originating* for example« from the mother liquors from the recrystallisation of a mixture of 5 diastereoisomeric salts. The chiral acid used for the separation of such an enriched mixture is then the antipode of that which made it possible to obtain the enriched mixture. Pharmacologically-acceptable acid addition 10 salts of the tetrahydronaphthalene derivatives of general formula (I)# e.g. methanesulphonates# mandelates# fumarates# maleates# malonates# citrates# hydrobromides and hydrochlorides# may be obtained by methods known per se, for example by treatment of the 15 tetrahydronaphthalene base with the appropriate acid in a solvent medium# e.g. an alkanol or ether# or mixtures thereof. By the term 'methods known per se' in this specification is meant methods heretofore used or 20 described in the literature. 201919 - n - The following Examples illustrate the preparation of compounds of general formula (I) of the invention. The analyses and the IR and NMR spectra confirm the structure of the compounds. EXAMPLE 1 2-Dipropylamino-5-formylamino-6-hydroxy- 1#2#3#4-tetrahydronaphthalene hydrobromide. (Rx = CHO# R2 = C3H7, R3 = C3H?, R4 = OH) (a) 2-Dipropylamino-6-methoxy-l# 2 # 3 #4-tetrahydronaphthalene. 20 g of 6-methoxytetrahydronaphthalen-2-one# 20 ml of dipropylamine and 200 mg of para-toluenesulphonic acid are introduced into 300 ml of benzene under a nitrogen atmosphere. The mixture, which has become black# is then heated under reflux for 12 hours# the water of condensation being removed by azeotropic distillation. The solution# which contains the compound (IV)# is then concentrated to a volume of about 100 ml. For the hydrogenation# 150 ml of ethanol and 300 mg of Pt02 are added thereto and hydrogenation is carried out# under a pressure of about 0.3 MPa# until the absorption has stopped. After removal of the catalyst# the solvents are driven off under reduced pressure and the residual black oil is taken up in toluene and extracted with N hydrochloric acid. The hydrochloric acid solution is then neutralised with an alkali and extracted with toluene# the organic phase is dried and filtered on 200 g of neutral alumina# and elution is completed by means of methylene 2019 1 - 12 - chloride. Concentration gives a virtually colourless oil. (b) 2-Dipropylamino-6-methoxy-5(and 7)-nitro-l,2,3,4-tetrahydronaphthalene. 5 21 g of 2-dipropylamino-6-methoxy-l,2,3,4- tetrahydronaphthalene are added to 60 ml of trifluoro-acetic acid* with simultaneous cooling of the mixture. 7 ml of nitric acid (d = 2.42) are then added dropwise, the temperature being kept at about 0°C. The mixture 10 is stirred for a further 10 minutes, the whole is poured into water and the Insoluble material is extracted with methylene chloride; the organic phase is shaken with a solution of potassium carbonate and washed with water. 15 After drying and evaporation, the brown gum obtained is subjected to chromatography on a column of neutral alumina (800 g), elution being carried out with toluene. The less polar compound is the isomer nitrated in the 5-position. 9 g of each of the isomers 20 are obtained. The compound nitrated in the 5-position melts at 198-220°C and the compound nitrated in the 7-position melts at 158-160°C (in the form of the hydrochlorides). (c) 2-Dipropylamino-6-hydroxy-5-nitro-l,2,3,4-25 tetrahydronaphthalene hydrobromide. 9 g of 2-dipropylamino-6-methoxy-5-nitro-1,2,3,4-tetrahydronaphthalene are introduced into - 13 - 100 ml of 48% hydrobromic acid and the mixture is heated under reflux for 2 hours. The acid is then driven off under reduced pressure and the residue is taken up three times in water, the water being evaporated off each time 5 in order to remove any trace of acid. When recrystallised from water, the solid obtained forms a monohydrate which melts at 236°C (with decomposition), (d) 2-Dipropylamino-5-amino-6-hydroxy-l,2,3,4-tetrahydronaphthalene hydrobromide. 10 7 g of 2-dipropylamino-6-hydroxy-5-nitro- 1,2,3,4-tetrahydronaphthalene hydrobromide are suspended in 250 ml of ethanol and hydrogenation is carried out at ambient temperature, in the presence of 1 g of 5% palladium-on-charcoal, under a pressure of about 0.3 MPa. 15 The solvent is then evaporated off and the residue is triturated in diethyl ether. The product obtained melts at 215-218°C (with decomposition). (e) 2-Dipropylamino-5-formylamino-6-hydroxy-l,2,3,4-tetrahydronaphthalene hydrobromide. 20 0.42 ml of acetic anhydride is added all at once to 2 ml of 98% formic acid, kept at 0°C, and the mixture is left at 0°C for 15 minutes. Then, still using an ice-bath, 1.34 g of 2-dipropylamino-5-amino-6-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide are introduced 25 therein with a spatula and the whole is stirred for one hour at 0°C. 7 019 19 - 14 - After diethyl ether has been added and the solid filtered off# the latter is recrystallised from the minimum amount of ethanol. This gives the title compound melting at 199°C. 5 EXAMPLE 2 2-Dipropylamino-7-formylamino-6-hydroxy- 1#2#3«4-tetrahydronaphthalene hydrobromide. (Rx = CHO# R2 = C3H7# R3 = C3H?, R4 = OH) (a) 2-Dipropylamino-7-amino-6-methoxy-l# 2#3«4-tetrahydronaphthalene. 10 9 g of the 2-dipropylamino-6-methoxy-7- nitro-1#2*3*4-tetrahydronaphthalene obtained in accordance with Example 1(b) are introduced into 200 ml of ethanol# together with 1 g of Raney nickel. At ambient temperature, hydrogenation is carried out under pressure 15 until the absorption has stopped. After evaporation of the solvent« an oil remains which is shown to oxidise fairly readily in air. (b) 2-Dipropylamino-7-amino-6-hydroxy-l# 2 #3#4-tetrahydronaphthalene dihydrobromide. 20 The product obtained above is introduced in 100 ml of 48% hydrobromic acid# the mixture is heated under reflux for 10 hours and the acid is then driven off under reduced pressure and subsequently removed completely by distillation with a toluene/ethanol 25 mixture in a rotary evaporator. After recrystallisation from isopropyl alcohol# the dihydrobromide melts at - 15 - 250°C (with decomposition). (c) 2-Dipropylamino-7-amino-7-hydroxy-l#2#3#4-tetrahydronaphthalene monohydrobromide. A solution of 5 ml of Amberlite LA2 resin in 5 50 ml of petroleum ether is added to a solution of 3 g of the dihydrobromide obtained in (b) above in 50 ml of water. The mixture is shaken for 15 minutes at ambient temperature and the aqueous phase is separated off and evaporated to dryness in order to isolate the crude monohydrobromide# 10 in an amorphous and coloured form* which is used as such for the formylation. (d) 2-Dipropylamino-7-formylamino-6-hydroxy-l#2# 3#4-tetrahydronaphthalene hydrobromide. 0.7 ml of acetic anhydride is added to 3 ml of 15 98% formic acid# kept at 0°C# and the whole is left for 15 minutes at 0°C. 2.2 g of 2-dipropylamino-7-amino-6-hydroxy-l#2,3# 4-tetrahydronaphthalene hydrobromide are then added thereto and the mixture is then stirred for one hour at 0°C. After 50 ml of diethyl ether 20 have been added and the solid has been filtered off# the latter is recrystallised from a 50/50 methanol/ethyl acetate mixture. This gives 1 g of the final product melting at 213°C (with decomposition). EXAMPLE 3 2-Dipropylamino-5-acetylamino-6-hydroxy-25 1#2#3#4-tetrahydronaphthalene hydrobromide. (Rx = COCH3# R2 = C3H7, R3 = C3H?# R4 = OH) 2 0 f>2 t! f - 16 - 10 ml of acetic acid and 0.46 ml of acetic anhydride are added to 1.5 g of 2-dipropylamino-5-amino-6-hydroxy-l# 2 # 3 #4-tetrahydronaphthalene hydrobromide (obtained in accordance with Example 1(d)) in 25 ml 5 of methylene chloride at 0°C. The mixture is stirred for one hour# diethyl ether is added and the solid is recrystallised from ethanol. This gives 1.2 g of a product melting at 244.5°C. EXAMPLE 4 2-Amino-6-hydroxy-7-formylamino-1#2#3»4-10 tetrahydronaphthalene hydrochloride. (Rx = CHO, R2 = H, R3 = H, R4 = OH) (a) 2-Amino-6-methoxy-l«2#3i4-tetrahydronaphthalene hydrochloride. A mixture of 10 g of 6-methoxytetrahydro-15 naphthalen—2-one in 150 ml of benzene and of 5.9 ml of benzylamine is heated under reflux for two hours with 100 mg of para-toluenesulphonic acid under a nitrogen atmosphere. The water of condensation is removed by azeotropic distillation. The mixture is concentrated to 20 a volume of 100 ml and subjected to catalytic hydrogenation# in the presence of 100 mg of Pt02# under a pressure of 0.3 MPa and at ambient temperature. The catalyst is removed by filtration and 4.7 ml of 12N hydrochloric acid are added to the filtrate. 25 A second hydrogenation is then carried out# in the presence of 1 g of palladium-on-charcoal# at about 60°C and at a pressure of the order of 0.35 MPa. Z019 1 9 - 17 - The catalyst is removed# the solvents are driven off under reduced pressure and the product formed is recrystallised from isopropyl alcohol; it melts at 254°C. 5 (b) 2-Acetylamino-6-methoxy-l#2#3#4-tetrahydronaphthalene . 2-Amino-6-methoxy-l#2 # 3#4-tetrahydronaphthalene hydrochloride is dissolved in a mixture of water and methylene chloride# and ION sodium hydroxide solution is 10 added thereto until the pH is 12. 1.5 equivalents of acetic anhydride are then added# the pH being kept between 10 and 12 with ION sodium hydroxide solution# and the mixture being cooled to about 15°C. The pH is then brought to between 7 and 8 and the organic phase is 15 separated off# dried and evaporated. When recrystallised from petroleum ether# the residue melts at 175°C. (c) 2-Acetylamino-7-nitro-6-methoxy-l# 2 #3 #4-tetrahydronaphthalene . 30 g of 2-acetylamino-6-methoxy-l#2#3«4-20 tetrahydronaphthalene are introduced in small amounts into 600 ml of nitric acid (d = 1.38)# the temperature being kept between -5 and -10°C. The reaction has ended when total dissolution has taken place. The solution is then poured into 2 litres of water and ice and the solid 25 is filtered off# washed and dried. This gives a mixture of the two mononitro isomers# the one being nitrated in ZD 1 9 1 18 the 5-position and the other in the 7-position, and of the dinitro compound. They are separated on a silica column with a 99/1 methyl ethyl ketone/methanol mixture. The compound nitrated in the 7-position melts at 175°C. 5 (d) 2-Acetylamino-7-amino-6-methoxy-l#2*3*4- melting at 158°C. 10 (e) 2#7-Diamino-6-hydroxy-l*2#3#4-tetrahydronaphthalene dihydrochloride. 2.7 ml of boron tribromide are added to a solution of 23 g of 2-acetamido-7-amino-6-methoxy-l#2#3#4-tetra-hydronaphthalene in methylene chloride at -60°C. The 15 mixture is left to return to ambient temperature# cooled to -60°C and neutralised with methanol. After evaporation to dryness# 12N hydrochloric acid is added and the mixture is heated under reflux for 48 hours. It is then left to cool and the crystals formed are filtered off# washed with 20 acetone and then with diethyl ether and dried. The product collected melts above 300°C. (f) 2-Amino-7-formylamino-6-hydroxy-1# 2 # 3 #4-tetrahydro- 25 resin in 50 ml of petroleum ether is added to a solution of 2 g of 2#7- diamino-6-hydroxy-l#2«3«4-tetrahydro- tetrahydronaphthalene. Hydrogenation under the conditions described in Example 2(a) gives* with a quantitative yield# a product naphthalene hydrochloride. A solution of 5 ml of Amberlite LA2 201 9 H S - 19 - naphthalene dihydrochloride in 50 ml of water. The mixture is stirred for 15 minutes at ambient temperature and the aqueous phase is collected and evaporated to dryness. This gives the monohydrochloride in a 5 quantitative yield. 0.83 ml of acetic anhydride is then added to 3 ml of formic acid in an ice-bath and the mixture is left for 15 minutes at 0°C. Still using the ice-bath# 1.69 g of the 2#7-diamino-6-hydroxy-l#2#3#4-tetrahydronaphthalene hydrochloride obtained as described 10 above are then added thereto and the mixture is stirred for a further one hour. After diethyl ether has been added and the solid has been filtered off# the latter is recrystallised from the minimum amount of ethanol. It melts at 235°C (with decomposition). 15 EXAMPLE 5 2-Dipropylamino-7-hydroxy-8-formylamino- 1« 2 # 3 #4-tetrahydronaphthalene hydrobromide. (R2 = CHO, R2 = C3H7, R3 = C3Hy# R4 = OH) (a) 2-Dipropylamino-7-methoxy-l«2 # 3 #4-tetrahydronaphthalene, A mixture of 20 g of 7-methoxytetrahydro- 20 naphthalen-2-one and 20 ml of dipropylamme m 200 ml of benzene is heated under reflux for 15 hours with 500 mg of para-toluenesulphonic acid# the water of condensation being distilled off. The benzene is then evaporated off and 100 ml of 25 ethanol and 500 mg of Pt02 are added. Hydrogenation is carried out at ambient temperature# under a pressure of 201919 - 20 - the order of 0.35 MPa, until the absorption has ended, the catalyst is removed, the alcohol is evaporated off, the product is poured into IN hydrochloric acid, the solution is washed with toluene, neutralised with an 5 alkali, extracted with toluene and dried. The organic phase thus obtained is filtered on neutral alumina, which is washed with toluene, and the filtrate is evaporated. 24 g of a colourless oil remain. (b) 2-Dipropylamino-8-nitro-7-methoxy-l,2,3,4-tetra-10 hydronaphthalene. The nitration of the product of (a) is carried out as in Example 1(b) and the two isomers are separated. The derivative nitrated in the 8-position is in the form of an oil. 15 (c) 2-Dipropylamino-8-amino-7-methoxy-l,2,3,4-tetrahydronaphthalene . The reduction is carried out as in Example 1(c). (d) 2-Dipropylamino-8-amino-7-hydroxy-l,2,3,4-tetra-20 hydronaphthalene dihydrobromide. The demethylation is carried out under the conditions of Example 2(b). The product obtained melts at 270°C (with decomposition). (e) 2-Dipropylamino-8-amino-7-hydroxy-l,2,3,4-tetra-25 hydronaphthalene hydrobromide. The dihydrobromide of the product of (d) is 2019 ! - 21 - treated with an Amberlite LA2 resin, as described above, to give the amorphous crude monohydrobromide, which is used as such. (f) 2-Dipropylamino-8-formylamino-7-hydroxyl-l,2,3,4-5 tetrahydronaphthalene hydrobromide. The formylation of the product of (c) is carried out under the same conditions as those described in Example 2(d). The title compound melts at 232.5°C. 10 EXAMPLE 6 2-Propylamino-6-hydroxy-5-formylamino- 1,2,3,4-tetrahydronaphthalene hydrobromide. (Rx = CHO, R2 = H, R3 = C3H?, R4 = OH) (a) 2-Propanoylamino-6-methoxy-l,2,3,4-tetrahydronaphthalene. 15 46 g of 2-amino-6-methoxy-l,2,3,4-tetrahydro naphthalene hydrochloride (prepared in accordance with Example 4(a)) are introduced into 200 ml of water and 300 ml of methylene chloride. The pH is adjusted to 12 with 10N sodium hydroxide solution. Then, with the 20 mixture in an ice-bath, 40 ml of propionic anhydride are added thereto, the pH being simultaneously kept at 12. The two phases which have formed are separated, the organic phase is dried and concentrated to dryness, the residue is taken up in diethyl ether, the mixture 25 is filtered and the material on the filter is dried. This gives 45 g of the acylated derivative, which melts at 125°C. - 22 - (b) 2-Propanoylamino-5-nitro-6-methoxy-l,2,3,4-tetrahydronaphthalene. 12.2 g of 2-propanoylamino-6-methoxy-l,2,3,4- i tetrahydronaphthalene are introduced into 100 ml of 5 trifluoroacetic acid, and 3 ml of nitric acid (d = 1.49) are added dropwise thereto. Stirring is continued for 8 hours and the mixture is then taken up in water and diethyl ether. To separate the nitro isomers, the mixture is subjected to chromatography under pressure, 10 on a silica column, elution being carried out with an 8/2 methylene chloride/ethyl acetate mixture. 5g of the isomer nitrated in the 7-position and 3.8 g of the isomer nitrated in the 5-position are finally collected. (c) 2-Propanoylamino-5-amino-6-methoxy-l,2,3,4-tetra-15 hydronaphthalene. 1.8 g of the isomer nitrated in the 5-position, prepared as described in (b) above, in suspension in 50 ml of methanol, are hydrogenated under the conditions of Example 1(d). After the catalyst has been filtered 20 off and the solvent has been evaporated off, 1.4 g of a product, melting at 141°C, are collected. (d) 2-Propylamino-5-amino-6-methoxy-l,2,3,4-tetrahydronaphthalene . 0.46 g of lithium aluminium hydride is intro-25 duced into 30 ml of tetrahydrofuran, a solution of 2.56 g of 2-propanoylamino-5-amino-6-methoxy-l,2,3,4- 20191 - 23 - tetrahydronaphthalene in 50 ml of tetrahydrofuran is then added and the mixture is heated under reflux for 24 hours. It is then cooled and hydrolysed with a 2N solution of sodium hydroxide, in an ice-bath. The 5 organic phase is separated off, dried and concentrated to dryness. After chromatography on silica with a 1/1 diethyl ether/methanol mixture, 1.8 g of a yellowish oil are collected. (e) 2-Propylamino-5-amino-6-hydroxy-l,2,3,4-tetra-10 hydronaphthalene hydrobromide. 50 ml of 48% hydrobromic acid containing 1.5 g of 2-propylamino-5-amino-6-methoxy-l,2,3,4-tetrahydronaphthalene are heated under reflux for 10 hours. 1.8 g of the dihydrobromide are then collected 15 by concentrating the reaction medium. By following the procedure of Example 2(c), 1.19 g of the monohydro-bromide are collected, melting at 280°C. (f) 2-Propylamino-5-formylamino-6-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide. 20 1.9 g of 2-propylamino-5-amino-6-hydroxy- 1,2,3,4-tetrahydronaphthalene hydrobromide are introduced into a mixture of 6 ml of formic acid and 0.67 ml of acetic anhydride, kept in an ice-bath for \ hour. The mixture is stirred for 3 hours at ambient temper-25 ature and then poured into diethyl ether. The precipitate which has formed is filtered off and washed with 2 Q 1 9 ? 9 - 24 - hot isopropyl alcohol. After drying, 1.7 g of the final compound are obtained, which melts at 210°C. EXAMPLES 7 to 23 Other compounds, prepared by analogous 5 methods, are illustrated in Table I below by indicating their structure and their physical properties. Table II illustrates the structures and physical properties of a few intermediates of 10 formulae VI and VII. TABLE I /R2 Example -NH-R^ r2 R3 R4 Melting Salt (x) point (°C) 1 (d) (5)-NH2 C3H7 C3H7 (6)-OH 215-218 HBr 1 (e) (5)-NH-CHO C3H7 C3H7 (6)-OH 199 HBr 2 (d) (7)-NH-CHO C3H7 C3H7 (6)-OH 213 HBr 3 (5)-NH-COCH3 C3H7 C3H7 (6)-OH 244-245 HBr 4 (e) (7)-NH2 H H (6)-OH 300 di-HCl 4 (f) (7)-NH-CHO H H (6)-OH 235 HC1 5 (f) (8)-NH-CHO C3H7 c3h7 (7)-OH 232.5 HBr 6 (e) (5)-NH2 H C3H7 (6)-OH 280 HBr 6 (f) (5)-NH-CHO H coh7 (6)-OH 210 HBr N> Ui NJ o vO TABLE I (continued) Rj^-NH y 2 Example -NH-R^ R2 r3 R4 Melting point (°C) Salt (x) 7 (7)-nh-coch3 c3h7 c3h7 (6)-OCH3 168-169 Mai 8 (7)-nh-coch3 c3h7 c3h7 (6)-oh 228-229 HBr 9 (7)-nh-cho h c3h7 (6)-oh 226 HBr 10 (7)-nh2 c2h5 c2h5 (6)-och3 208-209 hc1 11 (5)-nh2 c2h5 c2h5 (6)-och3 197-198 hcl 12 (5)-nh-cho c2h5 c2h5 (6)-och3 196-197 hc1 13 (7)-nh-cho c2h5 c2h5 (6)-och3 236-237 hcl 14 (7)-nh-cho coh. c9h. (6)-oh 199-200 HBr TABLE I (continued) Example -nh-r-l r2 r3 R4 Melting point (°C) Salt (x) 15 (7)-nh2 ch3 ch3 (6)-och3 134-135 Mai 16 (5)-nh2 ch3 ch3 (6)-och3 167-168 Mai 17 (7)-nh-cho ch3 ch3 (6)-och3 149-150 Mai 18 (5)-nh-cho ch3 ch3 (6)-och3 181-182 Mai 19 (7)-nh2 ch3 ch3 (6)-oh 227-228 HBr 20 (7)-nh-cho ch3 ch3 (6)-oh 217-218 HBr 21 (5)-nh-cho ch3 ch3 (6)-oh 264-265 HBr TABLE I (continued) r, RX-NH Example -NH-R1 R2 R3 R4 Melting point (°C) Salt (h) 22 (7)-NH-C0CH3 H H (6)-OH 228 HBr 23 (5)-NH-CHO H H (6)-OH >300 HBr 24 (5)-NH2 (5)-NH-CHO C3H7 C3H7 C3H7 C3H7 (6)-OH (6)-OH [«]25 .-32° [a]^s =-48° HBr HBr 25 (7)-NH2 (7)-NH-CHO C3H7 C3H7 C3H7 C3H7 (6)-OH (6)-OH l«725 =-70° D M/25 =-6 8° D H6r HBr l to 00 1 (a) HBr : hydrobromide HCl : hydrochloride Mai : maleate TABLE II R- /R2 Position of N02 r2 R3 r4 Melting point (°C) Salt 5 C3H7 C3H7 (6)-OCH3 198-200 HCl 7 C3H7 C3H7 (6)-OCH3 158-160 HCl 5 C3H7 C3H7 (6)-OH 236 HBr 5 ch3 ch3 (6)-och3 243-244 HCl 7 ch3 ch3 (6)-OCH3 240-241 HCl 5 C3H7 C3H7 (6)-OCH3 25 [<x]D =-140° HCl 7 C3H7 C3H7 (6)-OCH3 [aj^5 =-76° HCl l ro <£> N) O 2 019 19 - 30 - EXAMPLE 24 Enantiomers of 2-dipropylamino-5-formyl-amino-6-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide. (a) 2-Amino-6-methoxy-l,2,3,4-tetrahydro-5 naphthalene. The procedure of Example 4(a) is followed and the hydrochloride is converted to the base in a known manner, for example by evaporating the organic phase of a mixture of methylene chloride, water and 10 sodium hydroxide, into which the hydrochloride has been introduced. (b) Separation of the enantiomers of 2-amino-6-methoxy-1,2,3,4-tetrahydronaphthalene. A solution of 6 g of L(-)-dibenzoyltartaric 15 acid in 100 ml of ethanol is added rapidly to 5.5 g of the racemic amine (base), obtained as indicated above, in solution in 100 ml of ethanol. The heterogeneous - 31 - medium thus obtained is concentrated under reduced pressure, the concentrate is taken up in diethyl ether and, after filtration and drying, 11 g of a salt which contains ^ mol of L(-)-dibenzoyltartaric acid are 5 collected. This salt is recrystallised twice from ethanol containing 30% of water. The product obtained melts at 220-221°C. By converting it to the hydrochloride, an optically active salt is obtained which melts at 254°C (with decomposition) and has an optical 10 rotation of [a] = -73° (c—1, MeOH). To isolate the other enantiomer, the ethanolic mother liquors from recrystallisation of the L(-)-diben-zoyltartrate are concentrated, the base form of the 15 amine is re-formed and, after it has been extracted, the D(+)-dibenzoyltartrate thereof is precipitated by adding the corresponding acid. After recrystallisation/ the D(+)-dibenzoyltartrate melts at 220-221°C. By formation of the hydrochloride, an optically active salt is obtained 20 which has an optical rotation of [a]^5 = +73° (c=l, MeOH). (c) (-)-2-Dipropylamino-6-methoxy-l,2,3,4-tetrahydronaphthalene hydrochloride. 15 ml of a saturated solution of potassium 25 carbonate and then 9 ml of iodopropane are added to 1.9 g of the laevorotatory hydrochloride obtained as indicated 2019 19 32 above, in suspension in 20 ml of benzene. The mixture is stirred at the reflux temperature for 72 hours. The organic phase is then diluted with diethyl ether, and the hydrochloride is formed by adding a solution of hydrogen 5 chloride in diethyl ether and isolated in the usual manner. It melts at 154°C and has an optical rotation of (d) (-)-2-Dipropy1amino-5-formylamino-6-hydroxytetra-hydronaphthalene hydrobromide. [a] ^ = -2.2° (c=l, MeOH). 10 The procedure of Example 1(b), (c), (d) and (e) is followed, using the enantiomer prepared as indicated above instead of the racemic mixture The hydrochlorides of the intermediates nitrated in the 5-position and 7-position have 15 respective optical rotations of -140° and 25 D -76° (c=l, MeOH) The reduced intermediate hydrobromide (N^ in the 5-position) has an optical rotation of -32°C 20 (c=l, MeOH). - 33 - The hydrobromide of the final compound, which is the laevorotatory enantiomer of the compound prepared in accordance with Example 1, has an optical rotation of [a] =-48° ^ (c=l, MeOH). - 34 - The compounds of the invention were subjected to pharmacological tests which demonstrated their antihypertensive and antiparkinson activity. Thus, it was found that in rats or dogs 5 anaesthaetised with sodium pentobarbital, the blood pressure dropped markedly after intravenous injections of 10 to 100 yug/kg animal body weight. Furthermore, when administered intravenously or intraduodenally to dogs, the compounds of the 10 invention inhibit the responses to electric stimulations of the nictitating membrane and of the heart, their activity in this case being about 20 times greater than that of the known dopaminergic N,N-dipropyldopamine. The effects of the compounds of the invention 15 are blocked by the action of sulpiride, a known antagonist of dopamine. The antiparkinson activity of the compounds of the invention was demonstrated by the test for the antagonism towards the catalepsy induced by haloperidol. 20 It is known that, in rats, a certain number of neuroleptics induce a cataleptic state considered to be the reflection of a blocking of the dopaminergic receptors in the extrapyramidal system: this is the case of haloperidol, the cataleptigenic effect of 25 which is antagonised by the dopaminergic agonists such as apomorphine or amphetamine, by the tricyclic antidepressants and by the anticholinergics. 201919 - 35 - The method used in this case is a modification of that described by Tedeschi et al., Arch. Int. Pharmacodyn. (1959) 122, 129. The haloperidol is administered intra-5 peritoneally to the rats at a dose of 1 mg/kg animal body weight in a volume of 1 ml/100 g of body weight. Thirty minutes after this injection, the products to be studied are administered to 6 rats per dose and at a rate of 3 doses per product studied. 10 The catalepsy of the animals is evaluated 30 minutes (intraperitoneal administration) or 60 minutes (oral administration) after the administration of the product to be studied, and then every 30 minutes for 3 hours (intraperitoneal administration) or 4 hours 15 (oral administration). To do this, each animal is placed in a position such that each paw is resting on a "stopper" of 25 mm in height and 12 mm in diameter. The animal is considered to be cataleptic if it remains in this position for at least 10 seconds. 20 The average percentage of cataleptic animals, and then the percentage decrease relative to the control animals, are calculated for each dose and each product. The AD50, namely the dose which antagonises 25 the cataleptic effect of the haloperidol by 50%, is determined graphically. - 36 - It was thus found that the AD50 of the compounds of the invention was of the order of 7 mg/kg animal body weight, both by intraperitoneal administration and by oral administration. 5 Finally, their acute toxicity in mice is of the order of 90 mg/kg animal body weight, administered intravenously, and of the order of 150 mg/kg animal body weight, administered orally. Taking account of their properties, the 10 compounds of the invention can be used for the treatment of cardiovascular diseases, in particular for the treatment of hypertension, and also for the treatment of Parkinson's disease. They can be administered orally, rectally or parenterally in 15 daily doses of 1 to 500 mg per unit doses containing, for example, 1 to 100 mg of active substance. The invention includes pharmaceutical compositions containing, as active principle, the compounds of general formula (I), and their pharm-20 aceutically-acceptable acid addition salts, in association with any excipients suitable for their oral, rectal or parenteral administration. These pharmaceutical compositions can also contain other medicinal substances with which these compounds and 25 their salts are pharmaceutically and therapeutically compatible. </div>

Claims

1. 2 0 (9 - 37 - For oral administration, all the pharmaceutical forms suitable ibr this method of administration are used, that is to say tablets, coated tablets, gelatin capsules, capsules, cachets, and solutions and suspensions to be taken orally. For endorectal administration, suppositories are used. For parenteral administration, stabilised and buffered injectable solutions are used which are prepared in advance or for immediate use. 201 919 38 WHAT WE CLAIM IS: 1 .A 2-amino-l,2,3,4-tetrahydronaphthalene derivative in the form Of a raoemate or an enantiomer of the, general formula: wherein represents a hydrogen atom or an alkanoyl group containing from 1 to 4 carbon atoms, R2 and R3 each represent, independently of one another, a hydrogen atom or an alkyl group containing from 1 to 4 carbon atoms i and R^ represents a hydroxy or methoxy group located in the 6-position or 7-position, and pharrnacologically-acceptable acid addition salts thereof. to claim 1 wherein R^ represents a formyl or acetyl group and R2 and R^ each represent a propyl group, and pharmacologically-acceptable acid addition salts thereof. 8 1 N R1-NH

2.A tetrahydronaphthalene derivative according V 201919 - 39 -

3. a tetrahydronaphthalene derivative according to claim 1 wherein the group -NH-R^ is in the 5-position and R^ represents a formyl or acetyl group# R2 and R^ each represent a propyl group, and R4 represents a hydroxy or methoxy group located in the 6-position# and pharmacologically-acceptable acid addition salts thereof.

4. a tetrahydronaphthalene derivative according to claim 1 wherein the group -NH-R^ is in the 5-position and represents a formyl or acetyl group# R2 and R^ each represent a propyl group, and R^ represents a hydroxy group located in the 6-position, and pharmacologically-acceptable acid addition salts thereof.

5. - A tetrahydronaphthalene derivative according to claim 1 identified by reference to the formula in that claim in Table I hereinbefore included a's part of the Examples, and pharmacologically-acceptable acid addition salts thereof.

6. 2-DipropyjLamino-5-f ormylamino-6-hydroxy-1,2,3,4-tetrahydronaphthalene and its pharmacologically-acceptable acid addition salts.

7. A process for the preparation of a tetrahydronaphthalene derivative of the general formula depicted in claim 1, wherein -NR2R-j represents an amino or dialkylamino group, which is characterised in that a / l,2,3,4-tetrahydronaphthalen-2-one of the formula: 201919 - 40 - (II) (wherein the methoxy group is located in the 6-position or 7-position) is reacted with benzylamine or a dialkylamine of the general formula: R12~NH-R13 (III) (wherein R'^ and R'^ each represent an alkyl group containing from 1 to 4 carbon atoms), the compound obtained of the general formula: (IV) (wherein R"2 represents hydrogen and R" ^ represents a benzyl group, or both represent alkyl groups containing from 1 to 4 carbon atoms) is then hydrogenated to give a compound of the general formula: £N^ hi -ov 26JUU985 ml 20)919 - 41 - (wherein R"2 and R"^ both represent hydrogen atoms or both represent alkyl groups containing from 1 to 4 carbon atoms, and the methoxy group is located in the 6- or 7- position) of which the enanticniers are optionally separated when -NR'^R"^ represents a primary amino group, and of which the said primary amino group of one of the enantiorers or of the racemate is optionally dialkylated, then the compound of general formula (V) thus obtained is subjected to nitration and then to separation of the isomers to give a compound of the general formula: no2 then, if it is desired to obtain a compound of general formula (I) depicted in claim 1 wherein R4 represents the hydroxy group, the compound of general formula (VI) is demethylated resulting in a compound of the general formula: - 42 - , then the compound of general formula (VI) or (VII) is subjected to catalytic reduction with hydrogen to give a compound of the general formula: h2N (wherein R"2 and R"^ are as hereinbefore defined, and represents a hydroxy or methoxy group in the 6-position or 7-position) and finally, if desired, N-acvlation is carried out to give a compound of general formula (I) depicted in claim 1 wherein represents an alkanoyl group containing from 1 to 4 carbon atoms.

8. A process according to claim 7 characterised in that acylation of the amine of general formula (V) , wherein R"2 and R"^ both represent hydrogen atoms, is carried out before the nitration, and deacylation is carried out before the final acylation step.

9. - A process for the preparation of a tetrahydronaphthalene derivative of the general formula depicted in claim 1 wherein -NR^^ represents a monoalkylamino group, which is characterised in that a 1, 2,3,4-tetrahydronaphthalen-2-one of the formula: 10 \ 43 0 CHo0 (II) (wherein the methoxy group is located in the 6-position or 7-position) is reacted with benzylamine* hydrogenation is then carried out to give an amine of the general formula: (wherein NR'^R''^ represents -NT^)* then* if desired, the two enantiomers of formula (V) are separated* then the primary amino group of the racemate or of only one of the enantiomers is acylated by means of a acid (or an acylating derivative thereof) in which the number of carbon atoms corresponds to the length of the alkyl group R2 or of the compound of general formula (I) to be prepared* then the compound obtained is subjected to nitration, to separation of the isomers* to catalytic reduction with hydrogen and to reduction of the 2-alkanoylamino group with lithium aluminium hydride to a monoalkylamino group, then* if it is desired to obtain a compound of general formula (I) (V) - 44 - wherein represents the hydroxy group, the compound obtained is demethylated, and, finally, if desired, the NH2 group on the benzene ring of the resulting compound is acylated with an acid R'^-OH (wherein R1^ represents an alkanoyl group containing from 1 to 4 carbon atoms) or an acylating derivative thereof.

10. A process according to claim 7 or 9 characterised in that the separation of the enantiomers of a primary amine of general formula (V) is carried out by preparing the diastereoisomers of the salts which it forms with the antipodes of dibenzoyltartaric acid, and by separating the said diastereoisomers the tartrate anion being released.

11. A pharmaceutical composition characterised in that it contains, as active ingredient, a tetrahydronaphthalene derivative as claimed in any one of claims 1 to 6, or a pharmacologically-acceptable acid addition salt thereof, in association with a pharmaceutically-acceptable vehicle. «5'y ro-rHGifiPca By lirs/their authorised Agents., A. J. PARK & SON. P"r CD